Canonical Allele Identifier: PA916030989
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Val86Gly
CA340877
NM_001351297.2:c.257T>G